The increasing order of relative stabilities of the carbocations is given below:
This can be explained on the basis of
Updated On: Jul 7, 2022
electromeric effect of the methyl groups.
hyperconjugation effect of the methyl groups
-I effect of the methyl groups
none of these.
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The Correct Option isB
Solution and Explanation
Greater the number of alkyl groups attached to a positively charged carbon atom, greater is the hyperconjugation interaction and hence, greater is the stability of carbocations.